Heidary Zohreh, Zaki-Dizaji Majid, Saliminejad Kioomars, Khorramkhorshid Hamid Reza
Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
J Reprod Infertil. 2019 Apr-Jun;20(2):70-75.
The purpose of this study was to analyze the expression level of CRISP2, CATSPER1, PATE1 and SEMG1 genes in the sperm of men with asthenozoospermia (AZS). AZS is a cause of infertility in men in which the motility of the sperm is reduced. So far, a few genes have been associated with AZS; however, in most of the cases, its molecular etiology is unclear.
A total of 35 subjects with idiopathic AZS and 35 fertile and healthy men as control were included. In study after total RNA extraction and cDNA synthesis, relative quantification was performed. B2M was used as the normalizer gene and fold change was calculated by 2 method. Mann-Whitney test was used to compare the expression levels between the case and control groups with significance level of p<0.05.
Our results showed that CRISP2 (p=0.03) and SEMG1 (p=0.03) were significantly down-and up-regulated in AZS men respectively compared to the controls. But CATSPER1 and PATE1 did not show significant changes.
Down-regulation of CRISP2 and up-regulation of SEMG1 were associated with AZS, which could be suggested as the potential candidate genes for the development of a diagnostic marker or potentially for more studies for treatment of AZS.
本研究旨在分析弱精子症(AZS)男性精子中CRISP2、CATSPER1、PATE1和SEMG1基因的表达水平。AZS是男性不育的一个原因,其精子活力降低。到目前为止,已有少数基因与AZS相关;然而,在大多数情况下,其分子病因尚不清楚。
共纳入35例特发性AZS患者和35例生育力正常的健康男性作为对照。在研究中,提取总RNA并合成cDNA后进行相对定量。使用B2M作为标准化基因,并通过2-ΔΔCt方法计算倍数变化。采用Mann-Whitney检验比较病例组和对照组之间的表达水平,显著性水平为p<0.05。
我们的结果显示,与对照组相比,AZS男性中CRISP2(p=0.03)显著下调,SEMG1(p=0.03)显著上调。但CATSPER1和PATE1未显示出显著变化。
CRISP2的下调和SEMG1的上调与AZS相关,这可能被认为是开发诊断标志物的潜在候选基因,或者可能用于更多关于AZS治疗的研究。